rs9376092, LOC105378010

N. diseases: 10
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Chronic myeloproliferative disorder
CUI: C1292778
Disease: Chronic myeloproliferative disorder
47 0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 0.020 1.000 2 2017 2018
Polycythemia Vera
CUI: C0032463
Disease: Polycythemia Vera
38 0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 0.020 1.000 2 2015 2017
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 0.700 1.000 2 2009 2012
Thrombocythemia, Essential
CUI: C0040028
Disease: Thrombocythemia, Essential
37 0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 0.020 1.000 2 2015 2018
Corpuscular Hemoglobin Concentration Mean
4389 0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 0.700 1.000 1 2012 2012
Fetal hemoglobin determination
CUI: C0200695
Disease: Fetal hemoglobin determination
220 0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 0.700 1.000 1 2008 2008
Finding of Mean Corpuscular Hemoglobin
1206 0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 0.700 1.000 1 2012 2012
Hemoglobin E disease
CUI: C0238159
Disease: Hemoglobin E disease
4 0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 0.700 1.000 1 2010 2010
Mean corpuscular hemoglobin concentration determination
19 0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 0.700 1.000 1 2012 2012
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 0.700 1.000 1 2012 2012